This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.
|Medical Terms||Other Names||
|80%-99% of people have these symptoms|
|Abnormality of the ankles||0003028|
|Bilateral single transverse palmar creases||0007598|
Dislocations of the elbows
Elbow dislocations[ more ]
|Neurological speech impairment||
Speech impediment[ more ]
|Severe short-limb dwarfism||0008890|
Small thumbs[ more ]
Fused ankle bones
|30%-79% of people have these symptoms|
|Abnormally shaped carpal bones||
Abnormally shaped wrist bones
Abnormality of cognition
Mental impairment[ more ]
Short, cube shaped long bone of hand
Dislocation of hip[ more ]
Stiff joints[ more ]
|Percent of people who have these symptoms is not available through HPO|
|Distal femoral bowing||0005096|
|Hypoplasia of the radius||0002984|
|Hypoplasia of the ulna||0003022|
Small feet[ more ]
Short skankbone[ more ]
|Shortening of all middle phalanges of the fingers||
Shortened middle finger bones
|Shortening of all proximal phalanges of the fingers||
Shortening of all innermost bones of the fingers
|Single transverse palmar crease||0000954|
Making a diagnosis for a genetic or rare disease can often be challenging. Healthcare professionals typically look at a person’s medical history, symptoms, physical exam, and laboratory test results in order to make a diagnosis. The following resources provide information relating to diagnosis and testing for this condition. If you have questions about getting a diagnosis, you should contact a healthcare professional.
Living with a genetic or rare disease can impact the daily lives of patients and families. These resources can help families navigate various aspects of living with a rare disease.
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
New NCATS Rare Diseases Research Video
December 27, 2017
Rare Disease Day at NIH on March 1, 2018
December 19, 2017
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